Convergent chemoenzymatic synthesis of O-GalNAc rare cores 5, 7, 8 and their sialylated forms. Issue 7 (25th January 2023)
- Record Type:
- Journal Article
- Title:
- Convergent chemoenzymatic synthesis of O-GalNAc rare cores 5, 7, 8 and their sialylated forms. Issue 7 (25th January 2023)
- Main Title:
- Convergent chemoenzymatic synthesis of O-GalNAc rare cores 5, 7, 8 and their sialylated forms
- Authors:
- Gadi, Madhusudhan Reddy
Chen, Congcong
Bao, Shumin
Wang, Shuaishuai
Guo, Yuxi
Han, Jinghua
Xiao, Weidong
Li, Lei - Abstract:
- Abstract : Mucin rare cores 5, 7, and 8 with 1, 2-cis glycosidic bonds were prepared with exclusive stereo-selectivity from a versatile precursor. Enzyme-catalyzed regio-selective sialylation was then achieved, yielding natural sialylated rare cores. Abstract : All O -GalNAc glycans are derived from 8 cores with 2 or 3 monosaccharides linked via α- or β-glycosidic bonds. While chemical and chemoenzymatic syntheses of β-linked cores 1–4 and 6 and derived glycans have been well developed, the preparation of α-linked rare cores 5, 7, and 8 is challenging due to the presence of this 1, 2-cis linkage. Meanwhile, the biosynthesis and functional roles of these structures are poorly understood. Herein, we synthesize 3 α-linked rare cores with exclusive α-configuration from a versatile precursor through multifaceted chemical modulations. Efficient regioselective α2-6sialylion of the rare cores was then achieved by Photobacterium damselae α2-6sialyltransferase-catalyzed reactions. These structures, together with β-linked cores 1–4 and 6, and their sialylated forms, were fabricated into a comprehensive O -GalNAc core microarray to profile the binding of clinically important GalNAc-specific lectins. It is found that only Tn, (sialyl-)core 5, and core 7 are the binders of WFL, VVL, and SBA, while DBA only recognized (sialyl-)core 5, and Jacalin is the only lectin that binds core 8. In addition, activity assays of human α- N -acetylgalactosaminide α2-6sialyltransferases (ST6GalNAcTs)Abstract : Mucin rare cores 5, 7, and 8 with 1, 2-cis glycosidic bonds were prepared with exclusive stereo-selectivity from a versatile precursor. Enzyme-catalyzed regio-selective sialylation was then achieved, yielding natural sialylated rare cores. Abstract : All O -GalNAc glycans are derived from 8 cores with 2 or 3 monosaccharides linked via α- or β-glycosidic bonds. While chemical and chemoenzymatic syntheses of β-linked cores 1–4 and 6 and derived glycans have been well developed, the preparation of α-linked rare cores 5, 7, and 8 is challenging due to the presence of this 1, 2-cis linkage. Meanwhile, the biosynthesis and functional roles of these structures are poorly understood. Herein, we synthesize 3 α-linked rare cores with exclusive α-configuration from a versatile precursor through multifaceted chemical modulations. Efficient regioselective α2-6sialylion of the rare cores was then achieved by Photobacterium damselae α2-6sialyltransferase-catalyzed reactions. These structures, together with β-linked cores 1–4 and 6, and their sialylated forms, were fabricated into a comprehensive O -GalNAc core microarray to profile the binding of clinically important GalNAc-specific lectins. It is found that only Tn, (sialyl-)core 5, and core 7 are the binders of WFL, VVL, and SBA, while DBA only recognized (sialyl-)core 5, and Jacalin is the only lectin that binds core 8. In addition, activity assays of human α- N -acetylgalactosaminide α2-6sialyltransferases (ST6GalNAcTs) towards the cores suggested that ST6GalNAc1 may be involved in the biosynthesis of previously identified sialyl-core 5 and sialyl-core 8 glycans. In conclusion, we provide efficient routes to access α-linked O -GalNAc rare cores and derived structures, which are valuable tools for functional glycomics studies of mucin O -glycans. … (more)
- Is Part Of:
- Chemical science. Volume 14:Issue 7(2023)
- Journal:
- Chemical science
- Issue:
- Volume 14:Issue 7(2023)
- Issue Display:
- Volume 14, Issue 7 (2023)
- Year:
- 2023
- Volume:
- 14
- Issue:
- 7
- Issue Sort Value:
- 2023-0014-0007-0000
- Page Start:
- 1837
- Page End:
- 1843
- Publication Date:
- 2023-01-25
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2sc06925c ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 25967.xml